Gene: FRG2KP (FSHD region gene 2 family member K, pseudogene) Homo sapiens |
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Analyze |
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Symbol: |
FRG2KP |
Name: |
FSHD region gene 2 family member K, pseudogene |
RGD ID: |
10769293 |
HGNC Page |
HGNC:51797 |
Description: |
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Type: |
pseudo (Ensembl: lncRNA)
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RefSeq Status: |
VALIDATED |
Related Functional Gene: |
FRG2
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Latest Assembly: |
GRCh38 - Human Genome Assembly GRCh38 |
Position: |
Human Assembly | Chr | Position (strand) | Source | Genome Browsers |
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JBrowse | NCBI | UCSC | Ensembl |
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GRCh38 | 16 | 31,563,222 - 31,567,715 (-) | NCBI | GRCh38 | GRCh38 | hg38 | GRCh38 | GRCh38.p14 Ensembl | 16 | 31,563,082 - 31,564,783 (-) | Ensembl | GRCh38 | | hg38 | GRCh38 | GRCh38.p14 Ensembl | 16 | 31,563,185 - 31,567,716 (-) | Ensembl | GRCh38 | | hg38 | GRCh38 | GRCh37 | 16 | 31,574,543 - 31,579,036 (-) | NCBI | GRCh37 | GRCh37 | hg19 | GRCh37 | Cytogenetic Map | 16 | p11.2 | NCBI | | | | | HuRef | 16 | 29,134,368 - 29,168,536 (-) | NCBI | | HuRef | | | CHM1_1 | 16 | 32,893,192 - 32,897,685 (-) | NCBI | | CHM1_1 | | | T2T-CHM13v2.0 | 16 | 31,950,616 - 31,955,109 (-) | NCBI | | T2T-CHM13v2.0 | | |
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JBrowse: |
View Region in Genome Browser (JBrowse)
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Model |
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References
Genomics
miRNA Target Status
Predicted Target Of
Count of predictions: | 356 | Count of miRNA genes: | 305 | Interacting mature miRNAs: | 331 | Transcripts: | ENST00000565692, ENST00000568403 | Prediction methods: | Miranda, Rnahybrid | Result types: | miRGate_prediction | |
Expression
RNA-SEQ Expression
High: > 1000 TPM value
Medium: Between 11 and 1000 TPM
Low: Between 0.5 and 10 TPM
Below Cutoff: < 0.5 TPM
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alimentary part of gastrointestinal system |
circulatory system |
endocrine system |
exocrine system |
hemolymphoid system |
hepatobiliary system |
integumental system |
musculoskeletal system |
nervous system |
renal system |
reproductive system |
respiratory system |
sensory system |
adipose tissue |
appendage |
entire extraembryonic component |
High |
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Medium |
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300
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Low |
2
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3
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1
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1
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4
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2
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1
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2
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80
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6
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2
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Below cutoff |
457
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475
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264
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78
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286
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38
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647
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328
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378
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79
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216
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338
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41
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189
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405
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1
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Sequence
RefSeq Acc Id: |
ENST00000565692 |
Type: |
CODING |
Position: |
Human Assembly | Chr | Position (strand) | Source |
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GRCh38.p14 Ensembl | 16 | 31,563,185 - 31,567,716 (-) | Ensembl |
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RefSeq Acc Id: |
ENST00000568403 |
Type: |
CODING |
Position: |
Human Assembly | Chr | Position (strand) | Source |
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GRCh38.p14 Ensembl | 16 | 31,563,082 - 31,564,783 (-) | Ensembl |
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RefSeq Acc Id: |
NR_135055 |
RefSeq Status: |
VALIDATED |
Type: |
NON-CODING |
Position: |
Human Assembly | Chr | Position (strand) | Source |
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GRCh38 | 16 | 31,563,222 - 31,567,715 (-) | NCBI | CHM1_1 | 16 | 32,893,192 - 32,897,685 (-) | NCBI | T2T-CHM13v2.0 | 16 | 31,950,616 - 31,955,109 (-) | NCBI |
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Sequence: |
GTTGAAGAAGTGGCCAGAAAAAGAAAAGTATTTTGATGGCAGGCTGGAGAACATCATGAGAGTA AACTTTAGGCCTGTTGACTGTCATTTTGGCAATGTATTGGGCCCTGGCCAAAGTGCTTGGATGC AACGTGGGGCCAATCAATAAATCCATCCCCCATGCTTTTCCTGGCCATGAGGTAATCGGCAGCC TAGTTCATGTCTTGATGGGAACCTTTGCCATGTGGAAGGATCACATCTCAGGTTTCTTGACAAC TGGATGACTTTTGAGAACAAAGATCTAGGACAGATCTATTCTTGGATTGTGGACAGGCATCAGC CTACTAACATCATATGGAACAGGTCTCCTTTACAGAAAGGGGCTTGGATAAGGAGGAAAGACCA TCAGAAGAAAAGATAAGACACTGTCTTCTCATTCCAGTAAGAGCCACATGCAAGGCAAGAATCA GAGTCCAGCTCAGATGGGGGAACTCTAGGAAGAGAGAAATCCATTCCATGGACAGCTGCCAAGA TAGAGCAGGACAGCATCAAGGACATGAGCCGAAAGTGCAAAAGGACTGCTTGACTTTGGAAAAG AAACCAAAGGCCTCTCTGACACTGTACACATCAGTGAAATGAGGAGACCCATGATGCCTGCTGT GGGGGACCCCCAGAGGCCCACACCGGGCACAGCAAGCGGCCCAGATCTCAGTCTCTAGGAGACC ACCCACTGCCACTTCAGAAAAGCCTGGTGACCTCTCTGCACACTCCATCTGAAGCCATTTATCA CAACACAGCCCAGGTGTGGGAACAGTAGGCCTATTCTCTGCTGACCTGGGAGCAGCTGTCTGAG CTCACCCTGGCTCCAGGGGGACTCTGTGCTATGGTACAAACCTGTGCCGTGGCCGCCCAGATGG CCTATGTCTTTCCCACTGAGGGCTGGCTCATCCCAGC
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Additional Information
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